Search results for "Macromolecular Substance"

showing 10 items of 882 documents

Glycopolymer Functionalization of Engineered Spider Silk Protein-based Materials for Improved Cell Adhesion

2014

Silk protein-based materials are promising biomaterials for application as tissue scaffolds, due to their processability, biocompatibility, and biodegradability. The preparation of films composed of an engineered spider silk protein (eADF4(C16)) and their functionalization with glycopolymers are described. The glycopolymers bind proteins found in the extracellular matrix, providing a biomimetic coating on the films that improves cell adhesion to the surfaces of engineered spider silk films. Such silk-based materials have potential as coatings for degradable implantable devices.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsBiocompatibilityPolymer scienceGlycopolymerfungitechnology industry and agricultureBiomaterialBioengineeringNanotechnologymacromolecular substancesPolymerequipment and suppliesBiomaterialschemistry.chemical_compoundSILKchemistryMaterials ChemistrySurface modificationSpider silkCell adhesionBiotechnologyMacromolecular Bioscience
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Mechanical Characterization of Polysaccharide/polyaminoacid Hydrogels as Potential Scaffolds for Tissue Regeneration

2011

The mechanical properties of hydrogel scaffolds based on hyaluronic acid (HA) that were chemically crosslinked with α,β-poly(N-2-hydroxyethyl)(2-aminoethylcarbamate)-D,L-aspartamide (PHEA-EDA) were investigated. Variation of these properties as a function of three different PHEA-EDA amounts used to crosslink HA has been related to the reaction efficiency evaluated using a colorimetric assay. Moreover, the amount of unreacted amino groups that was still present in the hydrogels was related to the attachment behavior of human dermal fibroblasts to the hydrogel surface. The mechanical data and biological results suggest the suitability of the investigated hydrogels as scaffolds for the regener…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringRegeneration (biology)Organic Chemistrytechnology industry and agriculturemacromolecular substancesfibroblast attachment; hyaluronic acid; mechanical properties; polyaspartamide; scaffoldsPolysaccharidePolymer engineeringCharacterization (materials science)chemistry.chemical_compoundchemistryhyaluronic acid polyaspartamide scaffolds mechanical properties fibroblast attachment.Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoHyaluronic acidPolymer chemistrySelf-healing hydrogelsMaterials ChemistryBiophysics
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Polysiloxane-backbone block copolymers in a one-pot synthesis: a silicone platform for facile functionalization.

2012

Block copolymers consisting exclusively of a silicon-oxygen backbone are synthesized by sequential anionic ring-opening polymerization of different cyclic siloxane monomers. After formation of a poly(dimethylsiloxane) (PDMS) block by butyllithium-initiated polymerization of D3, a functional second block is generated by subsequent addition of tetramethyl tetravinyl cyclotetrasiloxane (D4(V) ), resulting in diblock copolymers comprised a simple PDMS block and a functional poly(methylvinylsiloxane) (PMVS) block. Polymers of varying block length ratios were obtained and characterized. The vinyl groups of the second block can be easily modified with a variety of side chains using hydrosilylation…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsMolecular StructureSiloxanesHydrosilylationOrganic Chemistrytechnology industry and agricultureSiliconesmacromolecular substancesPolymerRing-opening polymerizationPolymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationBlock (telecommunications)Polymer chemistryMaterials ChemistryCopolymerSide chainMacromolecular rapid communications
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Synthesis of well-defined polymeric activated esters

2008

Monomers bearing an activated ester group can be polymerized under various controlled polymerization techniques, such as ATRP, NMP, RAFT polymerization, or ROMP. Combining the functionalization of polymers via polymeric activated esters with these controlled polymerization techniques generate possibilities to realize highly functionalized polymer architectures. Within this highlight two different research areas of activated esters in polymer science will be discussed: (i) the preparation of defined reactive polymer architectures by controlled polymerization techniques and (ii) the preparation of defined reactive thin films. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureChain transfermacromolecular substancesPolymerChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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Synthesis of Functional Inorganic−Organic Hybrid Polymers Based on Poly(silsesquioxanes) and Their Thin Film Properties

2008

New stable and adherent coating materials have been synthesized on the basis of inorganic/organic hybrid polymers. As the inorganic part, different poly(silsesquioxanes) (PSSQ) have been functionalized to act as polymeric chain transfer agents (CTAs) for a reversible addition fragmentation chain transfer polymerization, thereby determining the starting point of a controlled radical polymerization of vinyl-type monomers. Using two different CTAs acrylates, we have successfully polymerized methacrylates and styrene under RAFT polymerization conditions. Different monomers were copolymerized in such an organic block to incorporate multiple functionalities. The variation of the block ratios and …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureChain transfermacromolecular substancesPolymerMethacrylateInorganic ChemistrySurface coatingPolymerizationchemistryPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationMacromolecules
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Amphiphilic poly(ether urethanes) carrying associative terpyridine side groups with controlled spacing

2021

The rational design of transiently crosslinked polymer gels requires a profound understanding of how molecular and topological factors determine the mechanical and dynamic material properties. To refine so-far established structure–property relations, complementary and versatile model sytems are still a crucial prerequisiste. In this study, the synthesis of a metallo-supramolecular associating terpyridine-diol (referred to as sticker) and its incorporation into poly(ethylene glycol) (pEG) based polyurethanes (PU) with strictly alternating vs. random sequences and variable sticker spacings is described. Synergetic effects resulting from the proximity of multiple neighboring urethane and stic…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRelaxation (NMR)technology industry and agricultureRational designBioengineeringEthermacromolecular substancesPolymerBiochemistrychemistry.chemical_compoundchemistryRheologyChemical engineeringAmphiphileTerpyridineEthylene glycolPolymer Chemistry
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Synthesis of polyvinyl acetate-graft-poly-2-oxazolines

1994

Poly(vinyl acetate-co-vinyl chloroformate) (1) was synthesized via phosgenation of poly(vinyl acetate-co-vinyl alcohol). It was shown that (1) is capable of initiating the polymerization of 2-phenyl-2-oxazoline and 2-methyl-2-oxazoline, when the counter ion is exchanged using potassium iodide. Polyvinyl acetate-graft-poly-2-phenyl-2-oxazoline and polyvinyl acetate-graft-poly-2-methyl-2-oxazoline are obtained in the grafting reaction.

chemistry.chemical_classificationMaterials sciencePolyvinyl acetatePolymers and Plasticsorganic chemicalsOrganic Chemistrytechnology industry and agriculturechemistry.chemical_elementAlcoholmacromolecular substancesChloroformateGraftingIodineRing-opening polymerizationchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCounterionPolymer International
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Chitin: A Structural Biopolysaccharide

2009

Chitin is a naturally occurring fibre-forming polymer that plays a protective role in many lower eukaryotes similar to that of cellulose in plants. Chemically it is a long-chain unbranched polysaccharide made of N-acetylglucosamine residues; it is the second most abundant organic compound in nature, after cellulose. Taking into account the structural role played by chitin, its metabolism (synthesis and degradation) is essential for different morphogenetic events. Absent in vertebrates and plants, chitin represents a parasite-specific target for chemotherapeutic attack and also plays a role in host immune responses. Because of its abundance in nature and its properties, biotechnological appl…

chemistry.chemical_classificationMaterials sciencebiologyCuticlefungimacromolecular substancesChitin synthasePolysaccharidecarbohydrates (lipids)ChitosanCell wallchemistry.chemical_compoundchemistryBiochemistryChitinChitinasebiology.proteinChitin nanofibrileLS
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Thermo- and light responsive micellation of azobenzene containing block copolymers

2010

In this communication, the synthesis and characterization of thermo- and light responsive block copolymers is reported. PEO-b-PNIPAM polymers with azobenzene moieties were prepared and analyzed by turbidimetry, fluorescence, NMR and DLS measurements. A temperature controlled reversible formation as well as a light induced disruption and reformation of micellar structures in water was found.

chemistry.chemical_classificationMaterials scienceeducationtechnology industry and agricultureMetals and Alloysmacromolecular substancesGeneral ChemistryPolymerFluorescenceCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundLight responsivechemistryAzobenzeneChemical engineeringPolymer chemistryMaterials ChemistryCeramics and CompositesLight inducedCopolymerTurbidimetryChemical Communications
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MCM-41 and related materials as media for controlled polymerization processes

1994

The synthesis of mesoporous MCM-41 type materials based on transition metal oxides and the polymerization of several monomers within MCM-41 is presented with the aim to specifically investigate the effects of the interface and confinement on host-guest interactions. In addition to standard MCM-41, material based on transition metal oxides is obtained although template removal has been unsuccessful for such compounds until now. In situ polymerization of styrene, methyl methacrylate and vinyl acetate is possible within the mesopore system. The properties of some of the encapsulated polymers differ markedly with those obtained in the bulk.

chemistry.chemical_classificationMaterials sciencemacromolecular substancesPolymerchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryVinyl acetateCoordination polymerizationIn situ polymerizationMethyl methacrylateIonic polymerizationMesoporous material
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